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上海恒遠(yuǎn)生物科技有限公司>>ELISA試劑盒>>ELISA試劑盒供應(yīng)商>>HY21317E人鳥苷酸交換因子(GEF)

人鳥苷酸交換因子(GEF)

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  • 型號(hào) HY21317E
  • 品牌 R&D/美國(guó)
  • 廠商性質(zhì) 生產(chǎn)商
  • 所在地 上海市

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上海恒遠(yuǎn)生物長(zhǎng)期供應(yīng)高質(zhì)量“人鳥苷酸交換因子(GEF) ",具有靈敏度高,操作方便,檢測(cè)速度快等優(yōu)點(diǎn),種屬齊全,現(xiàn)貨供應(yīng),物美價(jià)廉,提供完整的售前,售中售后服務(wù),歡迎各位新老客戶惠顧!

詳細(xì)介紹

上海恒遠(yuǎn)生物長(zhǎng)期提供酶免Elisa試劑盒、ELISA檢測(cè)試劑盒、免疫組化試劑盒、人Elisa試劑盒、大小鼠Elisa試劑盒、抗體抗原,價(jià)格實(shí)惠,質(zhì)量有保證,信譽(yù)*。凡購(gòu)買目錄本公司ELISA檢測(cè)試劑盒可免費(fèi)提供代測(cè)服務(wù)。更多Elisa試劑盒,咨詢:,.

試劑名稱:人鳥苷酸交換因子(GEF)

英文名稱:Human Guanine Exchange Factor,GEF ELISA KIT

檢測(cè)范圍:詳見(jiàn)說(shuō)明書

產(chǎn)品規(guī)格:96人份/48人份

檢測(cè)目標(biāo):人、大小鼠、豬、豚鼠、雞、羊、兔...

保存條件: 2-8℃

應(yīng)用范圍:科研用檢測(cè)試劑
人鳥苷酸交換因子(GEF)Assay procedure(操作步驟)
1.Dilute and add sample:Dilute Original density Standard as follow table:
8 pg/ml 5 Standard 150μl Original density Standard+150μl Standard diluent
4pg/ml 4 Standard 150μl 5 Standard+150μl Standard diluent
2 pg/ml 3 Standard 150μl 4 Standard+150μl Standard diluent
1 pg/ml 2 Standard 150μl 3 Standard +150μl Standard diluent
0.5 pg/ml 1 Standard 150μl 2 Standard +150μl Standard diluent
2.add sample:Set blank wells separay (blank comparison wells don’t add sample and HRP-
Conjugate reagent, other each step operation is same). testing sample well. add Sample
dilution 40μl to testing sample well, then add testing sample 10μl (sample final
dilution is 5-fold), add sample to wells , don’t touch the well wall as far as
possible, and Gently mix.
3.Incubate: After closing plate with Closure plate membrane ,incubate for 30 min at 37℃.
4.Configurate liquid: 30-fold wash solution diluted 30-fold (or 20-fold) with distilled
water and reserve.
5.washing:Uncover Closure plate membrane, discard Liquid, dry by swing, add washing buffer
to every well, still for 30s then drain, repeat 5 times, dry by pat.
6.add enzyme:Add HRP-Conjugate reagent 50μl to each well, except blank well.
7.incubate:Operation with 3.
8.washing:Operation with 5.
9.color:Add Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the
light preservation for 15 min at 37℃
10.Stop the reaction:Add Stop Solution50μl to each well, Stop the reaction(the blue color
change to yellow color).
11.assay:take blank well as zero , Read absorbance at 450nm after Adding Stop Solution
and within 15min.
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